Pular para o conteúdo
Merck
Todas as fotos(2)

Key Documents

View All Documentation

H9631

Sigma-Aldrich

DL-α-Hydroxystearic acid

≥99%

Sinônimo(s):

D,L-2-hydroxystearic acid, 2-Hydroxyoctadecanoic acid

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(2)

About This Item

Fórmula empírica (Notação de Hill):
C18H36O3
Número CAS:
629-22-1
Peso molecular:
300.48
Número MDL:
MFCD00046526
Código UNSPSC:
12352211
ID de substância PubChem:
24895861
NACRES:
NA.25

fonte biológica

synthetic (organic)

Ensaio

≥99%

forma

powder

grupo funcional

carboxylic acid

tipo de lipídio

saturated FAs

Condições de expedição

ambient

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CCCCCCCCCCCCCCCCC(O)C(O)=O

InChI

1S/C18H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(19)18(20)21/h17,19H,2-16H2,1H3,(H,20,21)

chave InChI

KIHBGTRZFAVZRV-UHFFFAOYSA-N

Categorias relacionadas

Ações bioquímicas/fisiológicas

DL-α-Hydroxystearic acid is a mixture of D and L-α-hydroxystearic acid (2-Hydroxyoctadecanoic acid) enantiomers. α-Hydroxystearic may be used in studies on the properties and metabolism of α-hydroxylated (2-hydroxylated) medium chain fatty acids.

Embalagem

Sealed ampule.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 8

1 of 8

Methyl 12-hydroxystearate ≥99% (GC)

Sigma-Aldrich

H7002

Methyl 12-hydroxystearate

Ricinoleic acid ≥95%

Sigma-Aldrich

R7257

Ricinoleic acid

12-Hydroxydodecanoic acid 97%

Sigma-Aldrich

198781

12-Hydroxydodecanoic acid

(±)-3-Hydroxydecanoic acid ≥98%

Sigma-Aldrich

H3648

(±)-3-Hydroxydecanoic acid

11-Hydroxyundecanoic acid 96%

Sigma-Aldrich

524395

11-Hydroxyundecanoic acid

15-Hydroxypentadecanoic acid 97%

Sigma-Aldrich

392979

15-Hydroxypentadecanoic acid

N,N-Dimetilformamida anhydrous, 99.8%

Sigma-Aldrich

227056

N,N-Dimetilformamida

γ-Linolenic acid ≥99%, liquid

Sigma-Aldrich

L2378

γ-Linolenic acid

Conrad D Lendrum et al.
Langmuir : the ACS journal of surfaces and colloids, 27(8), 4430-4438 (2011-03-23)
2-Hydroxyacids display complex monolayer phase behavior due to the additional hydrogen bonding afforded by the presence of the second hydroxy group. The placement of this group at the position α to the carboxylic acid functionality also introduces the possibility of
Samanta R Zanetti et al.
Biochimie, 92(12), 1778-1786 (2010-09-14)
Sphingolipids from rodent testis and spermatozoa are known to contain non-hydroxylated (N-) and 2-hydroxylated (2-OH) very-long-chain polyunsaturated fatty acids (VLCPUFA). In this study, the contribution of species with each type of fatty acids to the total ceramides (Cer) and sphingomyelins
S Sonnino et al.
Chemistry and physics of lipids, 69(2), 95-104 (1994-02-01)
GM1 ganglioside containing a hydroxylated fatty acid moiety, GM1(OH), was synthesized starting from lyso-GM1 and D-(+)-2-hydroxystearic acid. The aggregative, geometrical and distribution properties of GM1(OH) were compared with those of stearic acid containing GM1 ganglioside; laser light scattering measurements, differential
M Salim-Hanna et al.
Lipids, 24(8), 750-752 (1989-08-01)
Combined--but not individual--microsomal and supernatant fractions obtained from rat brains not only consume oxygen but also provoke emission from added chlorophyll. These results are consistent with literature data (Levis and Mead, J. Biol. Chem. 239, 77 [1964]) for trapping of
R Schütz et al.
International journal of cosmetic science, 41(3), 240-256 (2019-04-08)
We report on the preparation and efficacy of 10-hydroxystearic acid (HSA) that improves facial age spots and conspicuous pores. The hydration of oleic acid into HSA was catalyzed by the oleate hydratase from Escherichia coli. Following treatment with HSA, collagen
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica